Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Dimethyl perfluorohexanedioate | HCID 2737117 | — |
| Reactant | Red-Al | HCID 16684438 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20561441 | HCID 20561441 | — |
Reaction Steps
In a 3 liter three neck round bottom flask fitted with a mechanical stirrer, dropping funnel equipped with a drying tube, and low temperature thermometer was placed a solution of 50.0 g. (0.158 mol) of dimethyl perfluoroadipate in 450 ml. of dry tetrahydrofuran (THF). The reaction mixture was cooled to -70° C. (dry ice-acetone) and 67.5 ml. (0.238 mol.) of Vitride (70% in benzene) diluted with 50 ml. of THF was added dropwise over 30 min. with vigorous stirring. The temperature of the reaction was maintained at ≤-70° C. during the addition and at -70° C. for 2.5 hours after addition was complete. To the viscous mixture 500 ml. of 20% sulfuric acid previously chilled at 5° C. was added dropwise. The temperature of the reaction was allowed to rise to -50° C. and maintained until the excess Vitride had been decomposed. The mixture was then allowed to warm spontaneously to room temperature. Ether (400-600 ml.) was added with vigorous stirring until a homogeneous two-phase system was obtained. The layers were separated and the aqueous phase extracted with an additional 200-300 ml. of ether. The combined ether extracts were washed to neutrality with brine, dried over MgSO4, and evaporated under reduced pressure. The title compound was left as a thick syrup, 45.2 g. (96% by weight), νmaxneat 3600-2000 (bd) cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04302612 |
|---|
| Source dataset | uspto-grants-1981_11 |
|---|
| ORD ID | ord-0967c5262b024c9a9ec16d388c72caee |
|---|
| Source note | uspto-grants-1981_11 |
|---|